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Atomfair Ethyl 6-Bromopicolinate C8H8BrNO2

Description Ethyl 6-Bromopicolinate (CAS No. 21190-88-5) is a high-purity brominated pyridine derivative with the molecular formula C8H8BrNO2. This compound, also known as ethyl 6-bromopyridine-2-carboxylate , is a versatile building block in organic synthesis and pharmaceutical research. It features a reactive bromine substituent at the 6-position of the pyridine ring and an ester group at the 2-position, making it ideal for cross-coupling reactions, nucleophilic substitutions, and further functionalization. Our product is rigorously tested to ensure ??98% purity (HPLC/GC) and is supplied in sealed packaging under inert conditions to guarantee stability. Suitable for use in medicinal chemistry, agrochemical development, and material science…

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Description

Description

Ethyl 6-Bromopicolinate (CAS No. 21190-88-5) is a high-purity brominated pyridine derivative with the molecular formula C8H8BrNO2. This compound, also known as ethyl 6-bromopyridine-2-carboxylate, is a versatile building block in organic synthesis and pharmaceutical research. It features a reactive bromine substituent at the 6-position of the pyridine ring and an ester group at the 2-position, making it ideal for cross-coupling reactions, nucleophilic substitutions, and further functionalization. Our product is rigorously tested to ensure ??98% purity (HPLC/GC) and is supplied in sealed packaging under inert conditions to guarantee stability. Suitable for use in medicinal chemistry, agrochemical development, and material science applications.

  • CAS No: 21190-88-5
  • Molecular Formula: C8H8BrNO2
  • Molecular Weight: 230.06
  • Exact Mass: 228.97384
  • Monoisotopic Mass: 228.97384
  • IUPAC Name: ethyl 6-bromopyridine-2-carboxylate
  • SMILES: CCOC(=O)C1=NC(=CC=C1)Br
  • Synonyms: ethyl 6-bromopicolinate, 673-818-4, 21190-88-5, ethyl 6-bromopyridine-2-carboxylate, 6-Bromopyridine-2-carboxylic acid ethyl ester

Application

Ethyl 6-Bromopicolinate serves as a key intermediate in the synthesis of pharmaceuticals, ligands, and fine chemicals. It is widely used in Suzuki-Miyaura and Stille cross-coupling reactions to construct biaryl systems. Researchers employ it in the development of kinase inhibitors and other bioactive molecules due to its reactive bromine moiety. The ester group also allows for hydrolysis or transesterification to access carboxylic acid derivatives.

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